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41.
Carmen Attolini Giorgio Mazza Adriana Fortunato Giovanni Ciarrocchi Giorgio Mastromei Silvano Riva Arturo Falaschi 《Molecular & general genetics : MGG》1976,148(1):9-17
Summary The dnaP strains of Bacillus subtilis are altered in the initiation of DNA replication at high temperature (Riva et al., 1975). Fine mapping of the gene shows that it is located very close to the dnaF gene, described by Karamata and Gross (1970) and mapped by Love et al. (1976) in the polC region. The phenotype of both mutants is indistinguishable: the DNA synthesis stops at non permissive temperature after synthesizing an amount of DNA equivalent to the completion of the rounds of replication already initiated; at permissive temperature they are abnormally sensitive to MMS and are reduced in the ability to be transformed. Both mutants are to be considered as belonging to the dnaF locus.The dnaF gene is very close to the polC gene, which specifies the DNA polymerase III of B. subtilis. The DNA polymerase III of the dnaF mutants is not temperature sensitive in vitro, however, the level of this enzyme is lower by a factor of 4 or 5 in the dnaF mutants, at the permissive temperature. Following shift of dnaF cultures to the non permissive temperature, the level of DNA polymerase III activity specifically decreases further by a factor of at least 10 in the mutant, whereas the DNA polymerase I level is unaffected.The possible roles of the dnaF gene in the control of the cellular level of the DNA polymerase III, and the possibility of a regulatory role of DNA polymerase III in the initiation of DNA replication in bacteria are discussed.Abbreviations and symbols HPUra
6-(p-hydroxyphenylazo)-uracil; mic, minimum inhibitory concentration
- MMS
methyl-methanesufonate
- Pol I
Pol II and Pol III: DNA polymerase I, II and III respectively
- PCMB
parachloro-mercuri-benzoate 相似文献
42.
Fitzgerald JC Gao GP Reyes-Sandoval A Pavlakis GN Xiang ZQ Wlazlo AP Giles-Davis W Wilson JM Ertl HC 《Journal of immunology (Baltimore, Md. : 1950)》2003,170(3):1416-1422
In animal models, E1-deleted human adenoviral recombinants of the serotype 5 (AdHu5) have shown high efficacy as vaccine carriers for different Ags including those of HIV-1. Humans are infected by common serotypes of human adenovirus such as AdHu5 early in life and a significant percentage has high levels of neutralizing Abs to these serotypes, which will very likely impair the efficacy of recombinant vaccines based on the homologous virus. To circumvent this problem, a novel replication-defective adenoviral vaccine carrier based on an E1-deleted recombinant of the chimpanzee adenovirus 68 (AdC68) was developed. An AdC68 construct expressing a codon-optimized, truncated form of gag of HIV-1 induces CD8(+) T cells to gag in mice which at the height of the immune response encompass nearly 20% of the entire splenic CD8(+) T cell population. The vaccine-induced immune response provides protection to challenge with a vaccinia gag recombinant virus. Induction of transgene-specific CD8(+) T cells and protection against viral challenge elicited by the AdC68 vaccines is not strongly inhibited in animals preimmune to AdHu5 virus. However, the response elicited by the AdHu5 vaccine is greatly attenuated in AdHu5 preimmune animals. 相似文献
43.
Rafael Prados-Rosales Brian C. Weinrick Daniel G. Piqué William R. Jacobs Jr. Arturo Casadevall G. Marcela Rodriguez 《Journal of bacteriology》2014,196(6):1250-1256
Mycobacterium tuberculosis releases membrane vesicles packed with molecules that can modulate the immune response. Because environmental conditions often influence the production and content of bacterial vesicles, this study examined M. tuberculosis microvesicles released under iron limitation, a common condition faced by pathogens inside the host. The findings indicate that M. tuberculosis increases microvesicle production in response to iron restriction and that these microvesicles contain mycobactin, which can serve as an iron donor and supports replication of iron-starved mycobacteria. Consequently, the results revealed a role of microvesicles in iron acquisition in M. tuberculosis, which can be critical for survival in the host. 相似文献
44.
Chiliotrichiopsis peruviana Nesom, H. Rob. & Granda, a new species from Dept. Ayacucho in southwestern Peru, is described and illustrated. It is the
only rayless species of the genus, now expanded to four species, and the only one that occurs outside of Argentina.Chiliotrichiopsis is one of six shrubby South American genera of Astereae (subtribe Hinterhuberinae) with paleate receptacles. Observations
on morphology and a key to these genera provide perspective for the generic placement of the new species. 相似文献
45.
Fernando Díaz Herrera Elizabeth Sierra Uribe L. Fernando Bückle Ramirez Arturo Garrido Mora 《Journal of thermal biology》1998,23(6):381-385
1. Critical thermal maxima (CTMax) and minima (CTMin) were determined for postlarvae and juveniles of Macrobrachium rosenbergii acclimated at 20, 23, 26, 29 and 32±1°C. 2. At each acclimation temperature the CTMax and CTMin for postlarvae were 37.3, 38.3, 39.0, 41.0, 41.6°C and 10.0, 11.0, 13.0, 14.8, 16.8°C respectively and for juveniles 36.5, 38.4, 39.2, 41.5, 42.0 and 10.5, 11.3, 13.3, 14.6, 16.4°C respectively. 3. We found no indication of significant differences (P>0.05) in the CTMax and CTMin of the prawn postlarvae and juveniles. 4. The zone of thermal tolerance base on the CTMax and CTMin boundaries for postlarvae was 821.2°C2 and 816.9°C2 for juveniles, showing a high degree of eurythermality. To cultivate this species it should be done in no less than 16°C (CTMin) and below 42°C. 相似文献
46.
Cryptococcus neoformans capsular glucuronoxylomannan induces expression of fas ligand in macrophages 总被引:2,自引:0,他引:2
Monari C Pericolini E Bistoni G Casadevall A Kozel TR Vecchiarelli A 《Journal of immunology (Baltimore, Md. : 1950)》2005,174(6):3461-3468
The major component of capsular material of Cryptococcus neoformans is glucuronoxylomannnan (GXM), a polysaccharide that exhibits potent immunosuppressive properties in vitro and in vivo. The results reported here show that 1) soluble purified GXM induces a prompt, long-lasting, and potent up-regulation of Fas ligand (FasL) on macrophages, 2) the up-regulation of FasL is related to induced synthesis and increased mobilization to the cellular surface, 3) this effect is largely mediated by interaction between GXM and TLR4, 4) FasL up-regulation occurs exclusively in GXM-loaded macrophages, 5) macrophages that show up-regulation of FasL induce apoptosis of activated T cells expressing Fas and Jurkat cells that constitutively express Fas, and 6) anti-Fas Abs rescue T cells from apoptosis induced by GXM. Collectively our results reveal novel aspects of the immunoregulatory properties of GXM and suggest that this nontoxic soluble compound could be used to dampen the immune response, to promote or accelerate the death receptor, and to fix FasL expression in a TLR/ligand-dependent manner. In the present study, we delineate potential new therapeutic applications for GXM that exploit death receptors as key molecular targets in regulating cell-mediated cytotoxicity, immune homeostasis, and the immunopathology of diseases. 相似文献
47.
Genotype and allele frequencies of polymorphic cytochromes P450 CYP1A2 and CYP2E1 in Mexicans 总被引:3,自引:0,他引:3
Mendoza-Cantú A Castorena-Torres F Bermudez M Martínez-Hernández R Ortega A Salinas JE Albores A 《Cell biochemistry and function》2004,22(1):29-34
CYP1A2 and CYP2E1 are two of the main cytochrome P450 isoforms involved in the metabolism of commonly used drugs and xenobiotic compounds considered to be responsible for or possible participants in the development of several human diseases. Individual susceptibility to developing these pathologies relies, among other factors, on genetic polymorphism which depends on ethnic differences, as the frequency of mutant genotypes varies in different human populations. Thus the aim of this study was to investigate the frequency of CYP1A2 5'-flanking region and CYP2E1 Rsa I/Pst I polymorphisms in Mexicans by PCR-RFLP methods. The DNA of 159 subjects was analysed and mutant allele frequencies of 30% for CYP2E1 Rsa I/Pst I sites and 43% for CYP1A2 5'-flanking region were found. These frequencies are higher than those previously reported for other human populations. 相似文献
48.
The designation of a microbe as a potential biological weapon poses the vexing question of how such a decision is made given the many pathogenic microbes that cause disease. Analysis of the properties of microbes that are currently considered biological weapons against humans revealed no obvious relationship to virulence, except that all are pathogenic for humans. Notably, the weapon potential of a microbe rather than its pathogenic properties or virulence appeared to be the major consideration when categorizing certain agents as biological weapons. In an effort to standardize the assessment of the risk that is posed by microbes as biological warfare agents using the basic principles of microbial communicability (defined here as a parameter of transmission) and virulence, a simple formula is proposed for estimating the weapon potential of a microbe. 相似文献
49.
Eva Pericolini Elena Gabrielli Giovanni Bistoni Elio Cenci Stefano Perito Siu-Kei Chow Francesca Riuzzi Rosario Donato Arturo Casadevall Anna Vecchiarelli 《PloS one》2010,5(9)
Previously, we reported that Galactoxylomannan (GalXM) activates the extrinsic and intrinsic apoptotic pathways through an interaction with the glycoreceptors on T cells. In this study we establish the role of the glycoreceptor CD45 in GalXM-induced T cell apoptosis, using CD45+/+ and CD45−/− cell lines, derived from BW5147 murine T cell lymphoma. Our results show that whereas CD45 expression is not required for GalXM association by the cells, it is essential for apoptosis induction. In CD45+/+ cells, CD45 triggering by GalXM reduces the activation of Lck, ZAP70 and Erk1/2. Conversely, in CD45−/− cells, Lck was hyperphosphorylated and did not show any modulation after GalXM stimulation. On the whole, our findings provide evidence that the negative regulation of Lck activation occurs via CD45 engagement. This appears to be related to the capacity of GalXM to antagonize T cell activation and induce T cell death. Overall this mechanism may be responsible for the immune paralysis that follows GalXM administration and could explain the powerful immunosuppression that accompanies cryptococcosis. 相似文献
50.